An internal standard for the quantification of palmitic acid
Technical Support & Resources

Visit our FAQ

Contact Us

Toll Free Phone (USA and Canada Only): (888) 526-5351
Direct Phone: (734) 975-3888

Request Technical Support

Technical Support Request

To streamline the process attach the appropriate questionnaire to your inquiry.

Download IHC QuestionnaireDownload WB Questionnaire

View Our Privacy Statement for details on how we use and protect your data. In addition, this site is protected by hCaptcha and its Privacy Policy and Terms of Service apply.

Palmitic Acid-d9

Item No. 37061

Technical Information
Formal Name
hexadecanoic-13,13,14,14,15,15,16,16,16-d9 acid
CAS Number
1173022-49-5
Synonyms
  • C16:0-d9
  • Cetylic Acid-d9
  • FA 16:0-d9
  • Hexadecanoic Acid-d9
Molecular Formula
C16H23D9O2
Formula Weight
Purity
≥99% deuterated forms (d1-d9)
Formulation
A solid
DMF: 20 mg/mlDMSO: 20 mg/mlEthanol: 30 mg/ml
SMILES
[2H]C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])CCCCCCCCCCCC(O)=O
InChi Code
InChI=1S/C16H32O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16(17)18/h2-15H2,1H3,(H,17,18)/i1D3,2D2,3D2,4D2
InChi Key
IPCSVZSSVZVIGE-YNSOAAEFSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
Recommended Products

Certificates of Analysis & Batch Specific Data

Provide batch numbers separated by commas to download or request available product inserts, QC sheets, certificates of analysis, data packs, and GC-MS data.

    Add

    Add

    Add

    Lipid Resource Center
    Discover Products & Resources for Lipid Research
    • High-purity lipid standards
    • Lipid roles in biology
    • Lipids in health & disease
    • Lipids for pharmaceutical development
    • Protocols, advice, & resources
    EXPLORE NOW
    Product Description

    Palmitic acid-d9 is intended for use as an internal standard for the quantification of palmitic acid (Item No. 10006627) by GC- or LC-MS. Palmitic acid is a common 16-carbon saturated fat that represents 10-20% of human dietary fat intake and comprises approximately 25 and 65% of human total plasma lipids and saturated fatty acids, respectively.1,2 Acylation of palmitic acid to proteins facilitates anchoring of membrane-bound proteins to the lipid bilayer and trafficking of intracellular proteins, promotes protein-vesicle interactions, and regulates various G protein-coupled receptor functions.1 Palmitic acid (200 µM) increases NF-ĸB p65 levels, matrix metalloproteinase-9 (MMP-9) activity, and production of reactive oxygen species (ROS) in AsPC-1 pancreatic cancer cells, as well as increases migration of AsPC-1 cells.3 It increases COX-2 levels in RAW 264.7 cells and increases LPS-induced IL-1β levels and caspase-1 activity in isolated mouse peritoneal macrophages.4,5 Dietary administration of palmitic acid (2.2% w/w for 12 weeks) increases mouse hippocampal β-secretase 1 (BACE1) activity and amyloid-β (1-42) (Aβ42; Item No. 20574) levels.6 It also induces systolic contractile dysfunction in isolated mouse hearts.7 Red blood cell palmitic acid levels are increased in patients with metabolic syndrome compared to patients without metabolic syndrome and are also increased in the plasma of patients with type 2 diabetes compared to individuals without diabetes.8,9

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Fatima, S., Hu, X., Gong, R.-H., et alPalmitic acid is an intracellular signaling molecule involved in disease development. Cell. Mol. Life Sci. 76(13), 2547-2557 (2019).

    2. Santos, M.J., López-Jurado, M., Llopis, J., et alInfluence of dietary supplementation with fish oil on plasma fatty acid composition in coronary heart disease patients. Ann. Nutr. Metab. 39(1), 52-62 (1995).

    3. Binker-Cosen, M.J., Richards, D., Oliver, B., et alPalmitic acid increases invasiveness of pancreatic cancer cells AsPC-1 through TLR4/ROS/NF-κB/MMP-9 signaling pathway. Biochem. Biophys. Res. Commun. 484(1), 152-158 (2017).

    4. Lee, J.Y., Sohn, K.H., Rhee, S.H., et alSaturated fatty acids, but not unsaturated fatty acids, induced the expression of cyclooxygenase-2 mediated through Toll-like receptor 4. The Journal of Biological Chemisty 276(20), 16683-16689 (2001).

    5. Karasawa, T., Kawashima, A., Usui-Kawanishi, F., et alSaturated fatty acids undergo intracellular crystallization and activate the NLRP3 inflammasome in macrophages. Arterioscler. Thromb. Vasc. Biol. 38(4), 744-756 (2018).

    6. Marwarha, G., Rostad, S., Lilek, J., et alPalmitate increases β-site AβPP-cleavage enzyme 1 activity and amyloid-β genesis by evoking endoplasmic reticulum stress and subsequent C/EBP homologous protein activation. J. Alzheimers Dis. 57(3), 907-925 (2017).

    7. Knowles, C.J., Cebova, M., and Pinz, I.M. Palmitate diet-induced loss of cardiac caveolin-3: A novel mechanism for lipid-induced contractile dysfunction. PLoS One 8(4), e61369 (2013).

    8. Yi, L.-Z., He, J., Liang, Y.-Z., et alPlasma fatty acid metabolic profiling and biomarkers of type 2 diabetes mellitus based on GC/MS and PLS-LDA. FEBS Lett. 580(30), 6837-6845 (2006).

    9. Kabagambe, E.K., Tsai, M.Y., Hopkins, P.N., et alErythrocyte fatty acid composition and the metabolic syndrome: A National Heart, Lung, and Blood Institute GOLDN study. Clin. Chem. 54(1), 154-162 (2008).